Buccoliero Anna Maria, Caldarella Adele, Ammannati Franco, Mennonna Pasquale, Taddei Antonio, Taddei Gian Luigi
Dipartimento di Patologia Umana e Oncologia, Università degli Studi di Firenze, Italy.
Pathol Res Pract. 2002;198(9):627-33; discussion 635-8. doi: 10.1078/0344-0338-00312.
Neurocytoma is an unusual neuronal tumor especially affecting young people. It commonly arises in the ventricles and has a benign outcome. Herein, we report on a rare case of extraventricular neurocytomas (right parietal lobe) in a young girl admitted to hospital for a cranial trauma subsequent to a seizure. The tumor, radiologically well-circumscribed, cystic and enhancing, was surgically excised. The patient, who received no post surgical treatment, is alive and well after 18 months of follow-up. Pathological examination showed a well-differentiated lesion composed of uniform, round cells with perinuclear halos in a neuropil background and immunohistochemically positive for neuronal markers (synaptophysin, neuron-specific enolase, neurofilaments). The authors emphasize the role of the morphological and immunohistochemical evaluations to recognize this rare tumor.
神经细胞瘤是一种罕见的神经元肿瘤,尤其好发于年轻人。它通常起源于脑室,预后良好。在此,我们报告一例罕见的发生于脑室外(右顶叶)的神经细胞瘤,患者为一名年轻女孩,因癫痫发作后颅脑外伤入院。该肿瘤在影像学上边界清晰,呈囊性且有强化,经手术切除。该患者术后未接受治疗,随访18个月后仍存活且状况良好。病理检查显示为一个分化良好的病变,由均匀的圆形细胞组成,细胞周围有核周晕,位于神经纤维网背景中,免疫组化对神经元标志物(突触素、神经元特异性烯醇化酶、神经丝)呈阳性。作者强调了形态学和免疫组化评估在识别这种罕见肿瘤中的作用。